It is so hard to get a new diagnosis and cope with all that this means...I am so glad that you have sought out support...It is great the friends and family are trying to keep you involved and doing things outside the house, too. It is so easy to withdraw and that will not help you...
Do you have a good neuro who you feel comfortable with? This is so important and makes treatment easier. Ask that doctor how and whne you should communicate with him. (some allow email, others have you talk to a nurse, a few will call you back to talk with you) news things like new seizures or med side effects are usually things to check with him on....
I keep a journal of seizures, med side effects, problems that come up (suddenly not sleeping or sleeping too much, headaches, etc)
i also request copies of tests and reports and put it all in a 3 ring binder. This helps when they ask questions of me about all these tihngs and I cannot remember.....
Best wishes. I hope you find the med that works for you and support!